Effects on Gastroesophageal Reflux of Donkey Milk-Derived Human Milk Fortifier Versus Standard Fortifier in Preterm Newborns: Additional Data from the FortiLat Study

Nutrients. 2020 Jul 18;12(7):2142. doi: 10.3390/nu12072142.

Abstract

Background: Feeding intolerance is a frequent diagnosis in very preterm infants. As seen in the FortiLat trial, human milk fortification with the new donkey milk-derived human milk fortifier (DF) seems to improve feeding tolerance in these infants. The aim of this study was to evaluate the effects of using the DF compared with bovine milk-derived fortifier (BF) on gastroesophageal reflux (GER) in very low birth weight (VLBW) infants.

Methods: Over a total of 156 preterm infants were enrolled into the FortiLat trial (GA <32 weeks and birth weight <1500 g) and randomized into the BF arm or DF arm, and we selected all infants with clinical signs of GER and cardiorespiratory (CR) symptoms. All the infants underwent CR and multichannel intraluminal impedance and pH (MII/pH) monitoring associated with gastric ultrasound to evaluate GER and gastric emptying time.

Results: 10 infants were enrolled, and 5 were in the DF arm. At MII/pH, infants enrolled into the DF arm showed a lower GER frequency than BF arm infants (p = 0.036). Half gastric emptying time was similar in DF and BF arm infants (p = 0.744).

Conclusion: The use of donkey-derived human milk fortifier reduced the GER frequency and consequently should be recommended in infants with feeding intolerance.

Keywords: GORD; MII/pH; VLBW; cardiorespiratory events; feeding intolerance; tolerance; very preterm.

Publication types

  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Animals
  • Cattle
  • Equidae
  • Female
  • Food, Fortified*
  • Gastroesophageal Reflux / etiology
  • Gastroesophageal Reflux / prevention & control*
  • Humans
  • Infant
  • Infant Formula*
  • Infant Nutritional Physiological Phenomena / physiology*
  • Infant, Newborn
  • Infant, Very Low Birth Weight*
  • Male
  • Milk*
  • Milk, Human*